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      Li- and Na-reduction products of meso-Co3O4 form high-rate, stably cycling battery anode materials

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          Abstract

          A meso-porous Co 3O 4 has been found to retain its structure and cycle stably in a Li-ion or Na-ion battery.

          Abstract

          High surface area (367 m 2 g −1) meso-porous Co 3O 4 was investigated as the precursor of the anode material for lithium and also sodium ion batteries. Co 3O 4 is considered a potential anode material due to its theoretical capacity of 890 mA h g −1, over twice that of graphite. This comparatively higher capacity can be safely charged at rapid rates owing to a relatively high Li-insertion potentials, but, consequently, the discharged energy is yielded at an average potential near 2 V vs. Li/Li +, with full Li-extraction achieved over a continuum of potentials up to 3 V. The products of the lithium reduction of Co 3O 4 cycle stably from 0.01–3.0 V vs. Li/Li + with 600–900 mA h g −1 capacity retention at C rates from 1–5; the products of its sodium reduction cycle stably from 0.01–3.0 V vs. Na/Na + at C-rates up to 1 C with a lower 150–400 mA h g −1 capacity retention owing to greater ionic impedance. TEM, SAED and XRD were used to examine the cycled material and the stable performance is attributed to finding that the mesoporous structure is retained. Evaluation of five electrolyte formulations testing EC, FEC and Cl-EC showed that the stable meso-porous structure was best cycled with 5% FEC in EC:DEC at high charge/discharge rates, retaining 77% of its initial capacity at 5 C in a rate test. Comparison of the AC impedance spectra and of the XPS of the SEIs formed in the presence and in the absence of 5 vol% FEC shows that the SEI formed in the presence of FEC contains lithium fluoride and its carbonate layer is thinner than that formed in its absence, resulting in lesser impedance to Li migration through the SEI and facile ion de-solvation, improving the cycling performance. In cycling stability tests with EC:DEC, irregular cycling behaviour attributable to abrupt rises in cell resistance was regularly observed after testing over a few hundred cycles. Long-term cycling irregularities are inhibited by halogenated solvents and completely eliminated by adding fluoroethylene carbonate (FEC).

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          Graphene anchored with co(3)o(4) nanoparticles as anode of lithium ion batteries with enhanced reversible capacity and cyclic performance.

          We report a facile strategy to synthesize the nanocomposite of Co(3)O(4) nanoparticles anchored on conducting graphene as an advanced anode material for high-performance lithium-ion batteries. The Co(3)O(4) nanoparticles obtained are 10-30 nm in size and homogeneously anchor on graphene sheets as spacers to keep the neighboring sheets separated. This Co(3)O(4)/graphene nanocomposite displays superior Li-battery performance with large reversible capacity, excellent cyclic performance, and good rate capability, highlighting the importance of the anchoring of nanoparticles on graphene sheets for maximum utilization of electrochemically active Co(3)O(4) nanoparticles and graphene for energy storage applications in high-performance lithium-ion batteries.
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            Electrochemical Na Insertion and Solid Electrolyte Interphase for Hard-Carbon Electrodes and Application to Na-Ion Batteries

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              Virus-enabled synthesis and assembly of nanowires for lithium ion battery electrodes.

              The selection and assembly of materials are central issues in the development of smaller, more flexible batteries. Cobalt oxide has shown excellent electrochemical cycling properties and is thus under consideration as an electrode for advanced lithium batteries. We used viruses to synthesize and assemble nanowires of cobalt oxide at room temperature. By incorporating gold-binding peptides into the filament coat, we formed hybrid gold-cobalt oxide wires that improved battery capacity. Combining virus-templated synthesis at the peptide level and methods for controlling two-dimensional assembly of viruses on polyelectrolyte multilayers provides a systematic platform for integrating these nanomaterials to form thin, flexible lithium ion batteries.
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                Author and article information

                Journal
                JMCAET
                J. Mater. Chem. A
                J. Mater. Chem. A
                Royal Society of Chemistry (RSC)
                2050-7488
                2050-7496
                2014
                2014
                : 2
                : 34
                : 14209-14221
                Article
                10.1039/C4TA02684E
                903f35ee-6d7a-4f50-8518-5b00ed5740fa
                © 2014
                History

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